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Carbaryl

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Identification
Molecular formula
C12H11NO2
CAS number
63-25-2
IUPAC name
1-naphthyl N-methyl-N-nitroso-carbamate
State
State

At room temperature, carbaryl is solid.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
324.00
Boiling point (Kelvin)
597.15
General information
Molecular weight
201.22g/mol
Molar mass
201.2190g/mol
Density
1.2300g/cm3
Appearence

Carbaryl is a white crystalline solid with a mild odor. It can also be in powder form and is typically available in technical grade substances, which may be off-white to light tan.

Comment on solubility

Solubility of 1-naphthyl N-methyl-N-nitroso-carbamate

The solubility of 1-naphthyl N-methyl-N-nitroso-carbamate is a subject of interest due to its unique chemical structure and implications in various applications. This compound is known to exhibit variable solubility characteristics depending on several factors:

  • Polarity: The presence of the N-nitroso group influences its overall polarity, which can affect how well it dissolves in different solvents.
  • Solvent Type: It is generally more soluble in organic solvents, such as acetone or ethanol, as compared to water.
  • Temperature: Increased temperatures often enhance solubility, potentially aiding in achieving desired concentrations for practical use.
  • pH Levels: Changes in pH may impact the ionization state of the compound, leading to variations in solubility.

As stated in scientific literature, solubility can often be summarized as "the ability of a substance to dissolve in a solvent," and for 1-naphthyl N-methyl-N-nitroso-carbamate, understanding its solubility is crucial in fields such as pharmacology and toxicology. Optimizing its solubility may facilitate increased bioavailability and improve its efficacy in various applications. Therefore, experimenting with different conditions remains essential in unlocking the full potential of this compound.

Interesting facts

Interesting Facts about 1-naphthyl N-methyl-N-nitroso-carbamate

1-naphthyl N-methyl-N-nitroso-carbamate is a fascinating compound known for its intriguing chemical structure and potential applications. Below are some interesting insights into this compound:

  • Biological Activity: This compound has been studied for its potential biological activities, especially in relation to carcinogenicity. The nitroso functional group can play a significant role in the reactivity of the molecule, leading to interesting biochemical interactions.
  • Environmental Significance: Research has indicated that nitroso compounds often display environmental persistence. They can act as pollutants, affecting various ecosystems. Understanding their behavior in the environment is crucial for toxicological studies.
  • Synthesis: The synthesis of N-nitroso compounds typically involves the reaction of amines with nitrous acid. The process showcases classic organic reaction mechanisms and can provide insight into reaction conditions that enhance yield and selectivity.
  • Potential for Drug Development: Given the diverse biological activities associated with nitroso derivatives, 1-naphthyl N-methyl-N-nitroso-carbamate could be explored for potential medicinal use. The ongoing research in pharmacology could uncover novel therapeutic avenues.
  • Scientific Research: The compound has served as a subject for various research studies aimed at understanding the mechanisms of nitroso reactions and their impact on DNA. Such studies are vital for the comprehension of mutagenicity and carcinogenicity.

As we continue to study compounds like 1-naphthyl N-methyl-N-nitroso-carbamate, we deepen our knowledge of organic chemistry, toxicology, and environmental science. This aids in the development of better safety measures and novel applications in various fields.

Synonyms
Nitrosocarbaryl
N-Nitrosocarbaryl
Nitroso-nac
Denapon, nitrosated
1-Naphthyl methylnitrosocarbamate
1-Naphthyl N-methyl-N-nitrosocarbamate
7090-25-7
1-Naphthalenyl methylnitrosocarbamate
Methyl-nitrosocarbamic acid 1-naphthyl ester
CCRIS 1217
Denapon, nitrosated [Japanese]
N-Nitroso-1-naphthyl-N-methylcarbamate
Carbamic acid, methylnitroso-, 1-naphthalenyl ester
1-naphthyl-N-methyl-N-nitrosocarbamate
Carbamic acid, methylnitroso-, 1-naphthyl ester
BRN 1980650
C0719MRF0L
CARBAMIC ACID, N-METHYL-N-NITROSO-, 1-NAPHTHYL ESTER
CHEBI:189529
naphthalen-1-yl methyl(nitroso)carbamate
1-naphthalenyl N-methyl-N-nitrosocarbamate
N-methyl-N-nitrosocarbamic acid 1-naphthyl ester
NNitrosocarbaryl
1Naphthyl methylnitrosocarbamate
NNitroso1naphthylNmethylcarbamate
1Naphthyl NmethylNnitrosocarbamate
1Naphthalenyl methylnitrosocarbamate
Methylnitrosocarbamic acid 1naphthyl ester
Carbamic acid, methylnitroso, 1naphthyl ester
Carbamic acid, NmethylNnitroso, 1naphthyl ester
Carbamic acid, methylnitroso, 1naphthalenyl ester
Carbamic acid, methylnitroso, 1naphthalenyl ester (9CI)
Carbamic acid, methylnitroso-, 1-naphthalenyl ester (9CI)
1-Naphthyl methylnitrosocarbonate
UNII-C0719MRF0L
64158-97-0
Naphthalenyl methylnitrosocarbamate
naphthalen-1-yl N-methyl-N-nitrosocarbamate
Carbamic acid, methylnitroso-, naphthalenyl ester
DTXSID30876699
FFSXTYIBUNXZMF-UHFFFAOYSA-N
N-ME-N-NITROSO-1-NAPHTHYLCARBAMAT
1-Naphthyl 1-methyl-2-oxohydrazinecarboxylate #
Q27275003
Carbamic acid, N-methyl-N-nitroso-, 1-naphthalenyl ester